Aspire™ Audit

Protect Data Privacy and Enable Regulatory Compliance

Aspire™ Audit is an auditing solution designed and built for the clinical lifecycle, allowing your organization to demonstrate control and awareness of all activities associated with producing submission-ready deliverables.

Track activities and users who access your clinical artifacts in a user-friendly interface with dashboards, reports and ad-hoc queries providing your authorized users simple access to the information they need.


24/7 User Activity Monitoring	Configurable, Automated Reports	Robust Auditing of Users, Permissions, and File Events

Monitor and Protect

Aspire™ Audit provides 24/7 automated monitoring of clinical artifacts and a central point for querying and reporting the auditing data to clearly provide the who, what, and when supporting regulatory compliance.

Understand when members of your team:

Create, update, or delete files and folders
Create or change access to files and folders
Create, update, delete and change membership within permission groups
Submit analytical jobs (e.g. SAS and R)

Available Audit Collectors

Windows File Operations
Linux File Operations
Active Directory
Windows Local Security
Linux Background Code Execution
Windows Background Code Execution
Custom Operations

Track Changes With Ease

Review changes to folders, files or security permissions with Aspire™ Audit's user-friendly interface. Customize and automate flexible reports filtered by collector source, date, time or event type.

What Makes Instem Aspire™ Different?

Aspire™ is a cooperative framework built from individual Aspire™ software products. The configurable infrastructure of Aspire™ leverages transferable technologies that reduce the time and cost associated with customization and reinvention.

Aspire™ is built by Instem, the most trusted clinical technologists and business experts for data-science innovation.

Independent: Vendor, Software, and Language independence maximizes value to our clients
UX based design and prototyping
100+ Life Science, CRO & Medical Device Clients
95% Top 20 Global Pharma Clinical System Modernizations

We have a well-established track record of combining industry knowledge and technical expertise specific to the clinical trial lifecycle to deliver innovative solutions for our clients.

- Andy Ratcliffe,
Director, Technology Consulting